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AFACERI ŞI CONCURENŢĂ
AGRICULTURĂ, SILVICULTURĂ ŞI PESCUIT
ANGAJARE ÎN MUNCĂ ŞI CONDIŢII DE MUNCĂ
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Summary of European Union decisions on marketing authorisations in respect of medicinal products from 1 December 2020 to 31 December 2020 (Published pursuant to Article 13 or Article 38 of Regulation (EC) No 726/2004 of the European Parliament and of the Council)
Publicat(ă) la: 2021-01-29
Subiecte:
drug surveillance
,
EU Member State
,
market approval
,
marketing standard
,
medicament
,
veterinary medicinal product
,
withdrawal from the market
Author
Autor(i) colectiv(i):
Directorate-General for Health and Food Safety
(
Comisia Europeană
)
;
European Commission
Dreptul UE
PDF
HTML
Link permanent
Medicinal products – List of marketing authorisations granted by the EEA EFTA States for the first half of 2020 2021/C 39/04 Subcommittee I on the free movement of goods To be noted by the EEA Joint Committee
Publicat(ă) la: 2021-02-04
Subiecte:
EFTA countries
,
European Economic Area
,
free movement of goods
,
market approval
,
medicament
,
withdrawal from the market
Author
Autor(i) colectiv(i):
Standing Committee of the EFTA States
(
Asociația Europeană a Liberului Schimb
)
Dreptul UE
PDF
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Case C-488/20: Request for a preliminary ruling from the Wojewódzki Sąd Administracyjny w Warszawie (Poland) lodged on 2 October 2020 — Delfarma Sp. z o.o. v Prezes Urzędu Rejestracji Produktów Leczniczych, Wyrobów Medycznych i Produktów Biobójczych
Publicat(ă) la: 2020-10-02
Subiecte:
drug surveillance
,
drugs classification
,
import (EU)
,
import licence
,
import restriction
,
market approval
,
medicament
,
quantitative restriction
Author
Autor(i) colectiv(i):
Court of Justice
(
Curtea de Justiție a Uniunii Europene
)
Dreptul UE
PDF
HTML
Link permanent
Summary of European Union decisions on marketing authorisations in respect of medicinal products from 1 June 2020 to 30 June 2020 (Decisions taken pursuant to Article 34 of Directive 2001/83/EC or Article 38 of Directive 2001/82/EC)
Publicat(ă) la: 2020-07-31
Subiecte:
drug surveillance
,
EU Member State
,
market approval
,
marketing standard
,
medicament
,
withdrawal from the market
Author
Autor(i) colectiv(i):
Directorate-General for Health and Food Safety
(
Comisia Europeană
)
;
European Commission
Dreptul UE
PDF
HTML
Link permanent
Summary of European Union decisions on marketing authorisations in respect of medicinal products from 1 March 2019 to 31 March 2019 (Published pursuant to Article 13 or Article 38 of Regulation (EC) No 726/2004 of the European Parliament and of the Council 1 1 )
Publicat(ă) la: 2019-05-03
Subiecte:
drug surveillance
,
EU Member State
,
market approval
,
marketing standard
,
medicament
,
veterinary medicinal product
Author
Autor(i) colectiv(i):
European Commission
Dreptul UE
PDF
HTML
Link permanent
Summary of European Union decisions on marketing authorisations in respect of medicinal products from 1 January 2019 to 31 January 2019 (Decisions taken pursuant to Article 34 of Directive 2001/83/EC or Article 38 of Directive 2001/82/EC)
Publicat(ă) la: 2019-03-04
Subiecte:
drug surveillance
,
EU Member State
,
market approval
,
marketing standard
,
medicament
Author
Autor(i) colectiv(i):
European Commission
Dreptul UE
PDF
HTML
Link permanent
European Parliament resolution of 13 February 2019 on use of cannabis for medicinal purposes (2018/2775(RSP))
Publicat(ă) la: 2019-02-13
Subiecte:
drug addiction
,
drug surveillance
,
market approval
,
medical research
,
medicament
,
narcotic
,
research policy
,
scientific research
Author
Autor(i) colectiv(i):
Committee on the Environment, Public Health and Food Safety
(
Comisia PE
)
;
European Parliament
Dreptul UE
PDF
HTML
Link permanent
Case C-101/19: Request for a preliminary ruling from the Bundesverwaltungsgericht (Germany) lodged on 11 February 2019 — Deutsche Homöopathie-Union (DHU) Arzneimittel GmbH & Co. KG v Bundesrepublik Deutschland
Publicat(ă) la: 2019-02-11
Subiecte:
consumer information
,
labelling
,
medicament
,
pharmaceutical legislation
,
product designation
Author
Autor(i) colectiv(i):
Court of Justice
(
Curtea de Justiție a Uniunii Europene
)
Link permanent
European Parliament legislative resolution of 25 October 2018 on the proposal for a regulation of the European Parliament and of the Council amending Regulation (EC) No 726/2004 laying down Community procedures for the authorisation and supervision of medicinal products for human and veterinary use and establishing a European Medicines Agency (COM(2014)0557 – C8-0142/2014 – 2014/0256(COD))
Publicat(ă) la: 2018-10-25
Subiecte:
administrative expenditure (EU)
,
committee (EU)
,
delegated legislation
,
drug surveillance
,
European Medicines Agency
,
financial control
,
market approval
,
medicament
,
quasi-fiscal charge
,
rules of procedure
,
veterinary medicinal product
Author
Autor(i) colectiv(i):
European Parliament
Link permanent
Proposal for a REGULATION OF THE EUROPEAN PARLIAMENT AND OF THE COUNCIL amending Regulation (EC) No 469/2009 concerning the supplementary protection certificate for medicinal products
Publicat(ă) la: 2018-06-29
Subiecte:
administrative formalities
,
export (EU)
,
market approval
,
medicament
,
pharmaceutical legislation
,
public health
,
single market
Author
Autor(i) colectiv(i):
Directorate-General for Internal Market, Industry, Entrepreneurship and SMEs
(
Comisia Europeană
)
;
European Commission
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